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Change of E-cadherin by hepatocyte growth factor and effects on the prognosis of hypopharyngeal carcinoma.
DC Field | Value | Language |
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dc.contributor.author | Kim, CH | - |
dc.contributor.author | Kim, J | - |
dc.contributor.author | Kahng, H | - |
dc.contributor.author | Choi, EC | - |
dc.date.accessioned | 2011-03-10T01:40:57Z | - |
dc.date.available | 2011-03-10T01:40:57Z | - |
dc.date.issued | 2007 | - |
dc.identifier.issn | 1068-9265 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/1638 | - |
dc.description.abstract | BACKGROUND: Hepatocyte growth factor (HGF) is known to induce scattering in various epithelial cells, and E-cadherin plays important roles in the maintenance of cell-cell adhesion. However, the mechanisms surrounding these actions are not fully understood. Therefore, we examined how HGF affects the expression and distribution of E-cadherin. In addition, we observed the relationship between prognosis and modulation of E-cadherin by HGF in hypopharyngeal carcinoma.
METHODS: Tumor tissues from 66 patients with hypopharyngeal squamous cell carcinoma were evaluated for the expression of HGF, its receptor (c-Met), and E-cadherin. Reverse transcriptase-polymerase chain reaction (RT-PCR) and Western blot test were performed on hypopharyngeal cancer tissues. The association and changes of E-cadherin with HGF treatment in a hypopharyngeal cancer cell line were investigated by RT-PCR, Western blot analysis, inhibition assay, immunofluorescence staining, and invasion assay. RESULTS: E-cadherin expression was found in 87.9% of squamous cell carcinomas; these could be further classified as membranous type (46.9%) or nonmembranous type (53.1%). The expression of HGF in tumors with nonmembranous type E-cadherin expression was far higher than in tumors with membranous expression. Nonmembranous type E-cadherin expression correlated significantly with lymph node metastasis, distant metastasis, and recurrence (P < .05). HGF decreased the expression of E-cadherin and induced the translocation of E-cadherin to the cytoplasm. HGF and E-cadherin neutralizing antibody stimulated dispersion, and HGF significantly enhanced the invasion of hypopharyngeal cancer cells in a dose-dependent manner (P < .05). CONCLUSIONS: These results suggest that HGF can modulate the expression and intracellular localization of E-cadherin in hypopharyngeal cancer cells. In addition, these results indicate that changes in E-cadherin by HGF can affect the prognosis of hypopharyngeal carcinoma. | - |
dc.language.iso | en | - |
dc.subject.MESH | Adenocarcinoma | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Blotting, Western | - |
dc.subject.MESH | Cadherins | - |
dc.subject.MESH | Carcinoma, Squamous Cell | - |
dc.subject.MESH | Cell Proliferation | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Hepatocyte Growth Factor | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Hypopharyngeal Neoplasms | - |
dc.subject.MESH | Lymphatic Metastasis | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Neoplasm Invasiveness | - |
dc.subject.MESH | Neoplasm Recurrence, Local | - |
dc.subject.MESH | Neoplasm Staging | - |
dc.subject.MESH | Prognosis | - |
dc.subject.MESH | Proto-Oncogene Proteins c-met | - |
dc.subject.MESH | RNA, Messenger | - |
dc.subject.MESH | RNA, Neoplasm | - |
dc.subject.MESH | Reverse Transcriptase Polymerase Chain Reaction | - |
dc.subject.MESH | Tumor Cells, Cultured | - |
dc.subject.MESH | Tumor Markers, Biological | - |
dc.title | Change of E-cadherin by hepatocyte growth factor and effects on the prognosis of hypopharyngeal carcinoma. | - |
dc.type | Article | - |
dc.identifier.pmid | 17294073 | - |
dc.contributor.affiliatedAuthor | 김, 철호 | - |
dc.contributor.affiliatedAuthor | 김, 장희 | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.1245/s10434-006-9320-5 | - |
dc.citation.title | Annals of surgical oncology | - |
dc.citation.volume | 14 | - |
dc.citation.number | 5 | - |
dc.citation.date | 2007 | - |
dc.citation.startPage | 1565 | - |
dc.citation.endPage | 1574 | - |
dc.identifier.bibliographicCitation | Annals of surgical oncology, 14(5). : 1565-1574, 2007 | - |
dc.identifier.eissn | 1534-4681 | - |
dc.relation.journalid | J010689265 | - |
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